Literature DB >> 14007153

Hereditary nerve deafness. A follow-up of four cases in one family.

F WILLIAMS, L A ROBLEE.   

Abstract

Keywords:  DEAFNESS/genetics

Mesh：

Year:  1962        PMID： 14007153     DOI： 10.1001/archotol.1962.00740040073007

Source DB:  PubMed          Journal:  Arch Otolaryngol        ISSN： 0003-9977


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  3 in total

Review 1.  PROFOUND CHILDHOOD DEAFNESS.

Authors:  G R FRASER
Journal:  J Med Genet       Date:  1964-12       Impact factor: 6.318

2.  Histopathology of nonsyndromic autosomal dominant midfrequency sensorineural hearing loss.

Authors:  Fayez Bahmad; Jennifer O'Malley; Lisbeth Tranebjaerg; Saumil N Merchant
Journal:  Otol Neurotol       Date:  2008-08       Impact factor: 2.311

3.  Involvement of cochlin binding to sulfated heparan sulfate/heparin in the pathophysiology of autosomal dominant late-onset hearing loss (DFNA9).

Authors:  Tomoko Honda; Norihito Kawasaki; Rei Yanagihara; Ryo Tamura; Karin Murakami; Tomomi Ichimiya; Naoki Matsumoto; Shoko Nishihara; Kazuo Yamamoto
Journal:  PLoS One       Date:  2022-07-28       Impact factor: 3.752
  3 in total

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